ENST00000258385.8:c.1200G=
MANE Select
|
ENSP00000258385.3:p.Met400=
|
|
ENST00000258385.7:c.1200G=
|
ENSP00000258385.3:p.Met400=
|
|
ENST00000441621.6:c.*382G=
|
ENSP00000408819.2:n.*382G=
|
|
ENST00000446616.1:c.*841G=
|
ENSP00000410801.1:n.*841G=
|
|
ENST00000543200.5:c.1155G=
|
ENSP00000438380.1:p.Met385=
|
|
NM_000751.2:c.1200G=
|
NP_000742.1:p.Met400=
|
|
NM_001256657.1:c.1155G=
|
NP_001243586.1:p.Met385=
|
|
NM_001311195.1:c.618G=
|
NP_001298124.1:p.Met206=
|
|
NM_001311196.1:c.897G=
|
NP_001298125.1:p.Met299=
|
|
NR_046333.1:c.-4294966351G=
|
|
|
NR_046334.1:c.-4294966072G=
|
|
|
XM_011510524.1:c.819G=
|
XP_011508826.1:p.Met273=
|
|
XM_011510524.2:c.819G=
|
XP_011508826.1:p.Met273=
|
|
NM_000751.3:c.1200G=
MANE Select
|
NP_000742.1:p.Met400=
|
|
NM_001311195.2:c.618G=
|
NP_001298124.1:p.Met206=
|
|
NM_001311196.2:c.897G=
|
NP_001298125.1:p.Met299=
|
|
NM_001256657.2:c.1155G=
|
NP_001243586.1:p.Met385=
|
|